US11905245B2ActiveUtilityA1
Heterocyclic compound and organic light emitting device comprising the same
Est. expiryDec 3, 2038(~12.4 yrs left)· nominal 20-yr term from priority
C07D 209/82C07D 215/04C07D 215/12H10K 85/40H10K 85/615H10K 85/631H10K 85/6572H10K 50/11H10K 85/626C07D 403/04C07F 7/0814
53
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Claims
Abstract
The present disclosure relates to a novel heterocyclic compound represented by the following Chemical Formula 1 and to an organic light emitting device comprising the same:wherein, R1, R2, R3, R4, R5, R6, m, n and o are described herein.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1. A compound represented by the following Chemical Formula 1:
in the Chemical Formula 1,
R 1 is a substituted or unsubstituted C 6-60 aryl,
R 2 and R 3 are each independently a substituted or unsubstituted C 3-10 cycloalkyl; a substituted or unsubstituted C 6-60 aryl; a substituted or unsubstituted C 6-60 arylamine; or a substituted or unsubstituted C 5-60 heteroaryl containing one or more hetero atoms selected from the group consisting of N, O, S and Si; or —Si(A 1 )(A 2 )(A 3 ), wherein A 1 , A 2 and A 3 are each independently a substituted or unsubstituted C 1-60 alkyl; a substituted or unsubstituted C 3-10 cycloalkyl; a substituted or unsubstituted C 6-60 aryl; a substituted or unsubstituted C 5-60 heteroaryl containing one or more hetero atoms selected from the group consisting of N, O, S and Si; a monovalent non-aromatic condensed polycyclic group; or a monovalent non-aromatic hetero-condensed polycyclic group,
R 4 and R 5 are each independently hydrogen; deuterium; halogen; or a substituted or unsubstituted C 1-60 alkyl,
R 6 is hydrogen; or deuterium,
m and o are each independently an integer of 0 to 3, and
n is an integer of 0 to 4.
2. The compound of claim 1 ,
wherein the compound represented by Chemical Formula 1 is a compound represented by the following Chemical Formula 2 or Chemical Formula 3:
wherein, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , m, n and o are as defined in claim 1 .
3. The compound of claim 1 ,
wherein R 1 is phenyl; biphenylyl; terphenylyl; quarterphenylyl; naphthyl; phenanthrenyl; chrysenyl; fluoranthenyl; pyrenyl; or triphenylenyl.
4. The compound of claim 1 ,
wherein R 2 and R 3 are each independently any one selected from the group consisting of:
wherein,
R′ are each independently hydrogen; deuterium; halogen; or a substituted or unsubstituted C 1-60 alkyl, and
each p is independently an integer of 0 to 3.
5. The compound of claim 4 ,
R′ is hydrogen; or C 1-10 alkyl.
6. The compound of claim 1 ,
wherein R 4 and R 5 are each independently hydrogen; deuterium; methyl; ethyl; propyl; n-propyl; isopropyl; butyl; n-butyl; isobutyl; or tert-butyl.
7. The compound of claim 1 ,
wherein the compound represented by Chemical Formula 1 is any one selected from the group consisting of:
8. An organic light emitting device comprising: a first electrode; a second electrode that is provided opposite to the first electrode; and one or more organic material layers that are provided between the first electrode and the second electrode, wherein at least one layer of the organic material layers includes the compound according to claim 1 .
9. The organic light emitting device of claim 8 ,
wherein the at least one layer of the organic material layers including the compound is a light emitting layer.Cited by (0)
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